The Efficacy and Safety of Different Doses of SY-004 in Patients With Type 2 Diabetes Mellitus

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Suzhou Yabao Pharmaceutical R&D Co., Ltd.
Updated on 19 February 2024
fasting
antidiabetic agents
fasting blood glucose
antidiabetic agent
blood glucose self-monitoring
monitors blood glucose

Summary

This is a multicenter, randomized, double-blind, placebo-controlled phase II clinical study in patients with type 2 diabetes mellitus (T2DM).

Description

200 cases will be included and divided into four groups with 50 cases in each group

Details
Condition NIDDM, Diabetes Mellitus
Age 18-75 years
Treatment SY-004, SY-004 matching placebo
Clinical Study IdentifierNCT04217291
SponsorSuzhou Yabao Pharmaceutical R&D Co., Ltd.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Gender is not limited
Age at screening: 18 years old, 75 years old
According to WHO diagnostic criteria and classification in 1999, type 2 diabetes was diagnosed, with a course of at least 3 months
During screening and before randomization, 18kg / m2 BMI 35kg / m2
At the time of screening, they had been treated with diet or exercise for at least 3 months
No antidiabetic drugs were used at the time of screening, or the antidiabetic drugs were used irregularly within 3 months before screening (the cumulative use of antidiabetic drugs in the past 3 months was no more than 2 weeks and no antidiabetic drugs were used in the past 1 month)
During screening, 7% of the samples detected by local laboratory were HbA1c 11%
Before randomization, the central laboratory tested 7% HbA1c 11%
Fasting blood glucose (FBG) of 7-13.3 mmol / L (including boundary value) was measured in the central laboratory before randomization
The subjects must have informed consent before the study, and signed the written informed consent voluntarily
The subjects were willing and able to use the home blood glucose meter for self blood glucose monitoring
The subjects were able to communicate well with the researchers and complete the study according to the protocol

Exclusion Criteria

Staff members and their immediate family members of the research project. Lineal relatives refer to persons with consanguineous or legal relationships, including spouses, parents, children, brothers and sisters
Any of the following drugs or treatments were used prior to screening
In the past six months, insulin therapy has been used for more than one month, or insulin therapy is needed at present
Long acting GLP-1 has been used in the past 6 months
Glucokinase activator (GKA) was used in the past 6 months
In the past 6 months, I have received weight-loss drugs or any weight-loss treatment (such as surgery, excessive diet and exercise therapy) that leads to weight instability
Participated in clinical trials of any drug or medical device in the past 3 months
Other drugs that may affect blood glucose metabolism have been used in the past 8 weeks, including growth hormone treatment, and long-term or repeated intermittent systemic glucocorticoids (intravenous, oral or intra-articular administration for more than 2 weeks or repeated courses, except inhalation or local external use), etc
Strong CYP3A inducers or strong CYP3A inhibitors have been used in the past two weeks or are planned to be used in the near future (refer to appendix 12.5.1)
Drugs that are likely to cause torsade de pointes have been used in the past two weeks or planned in the near future (refer to appendix 12.5.2)
Prior to screening, there was a history or evidence of any of the following diseases
Type 1 diabetes, special type diabetes and secondary diabetes
Significant clinical cardiovascular events have occurred in the past 6 months (refer to appendix 12.3)
Patients with clinically significant peripheral vascular lesions, such as ischemic ulcer or gangrene, diabetic foot ulcer and infection
There is sufficient evidence for the presence of active diabetic proliferative retinopathy or maculopathy that is unstable or in need of treatment
there are obvious autonomic neuropathy, such as urinary retention, orthostatic hypotension, diabetic diarrhea or gastroparesis
Have a history of acute or chronic pancreatitis
Ketoacidosis, diabetic acidosis or hyperosmolar nonketotic coma have occurred in the past 6 months and need to be hospitalized
In the past 6 months, serious hypoglycemic events with unknown causes (need other people's help to recover); or frequent hypoglycemia: for example, more than two hypoglycemic events (blood glucose 3.9mmol / L) occurred in the first month before screening
Any endocrine system disease related to blood glucose (such as hyperthyroidism, acromegaly, Cushing's syndrome), immune system disease or other diseases that are unstable or need treatment are not suitable for the study according to the judgment of researchers
Have other diseases that affect glucose metabolism or are taking drugs that significantly affect glucose metabolism
Severe trauma or acute infection that may affect blood glucose control has occurred in the past month
Suffer from serious cardiovascular disease, respiratory system disease, gastrointestinal disease, liver dysfunction, renal dysfunction, endocrine disease (except diabetes), blood system disease, nervous system disease, and the disease status can significantly change the absorption, distribution, metabolism and excretion of the test drug, or taking the test drug will increase the risk of the subject or affect the analysis of the research results
There are any types of malignant tumors (whether cured or not)
A history of diseases that may cause hemolysis or red blood cell instability that affect HbA1c detection, such as hemoglobinopathy (such as sickle cell anemia or thalassemia, ferriblastic anemia)
History of alcohol and drug abuse. Drink more than 21 units (male) or 14 units (female) of alcohol per week (1 unit is about 360 ml of beer or 45 ml of spirits or 150 ml of wine with 40% alcohol)
There are mental or nervous system diseases, unwillingness to communicate or language barriers, and insufficient understanding and cooperation
There is any laboratory inspection index meeting the following standards at screening or random
In the absence of pacemaker, 12 lead ECG showed second or third degree atrioventricular block, or corrected qtcb > 450ms (male) or > 470ms (female)
eGFR<60ml/(min1.73m2)
ALT > 1.5 times the upper limit of normal value ( ULN), AST > 1.5 ULN, TBIL > 1.5 ULN
Hypertension (systolic blood pressure 160mmhg or diastolic blood pressure 100mmhg) that cannot be controlled by drugs or other treatment means exists
Hypertriglyceridemia (triglyceride > 500mg / dl (5.70mmol / L)) was found which could not be controlled by drugs or other treatments
Hemoglobin < 90g / L
The serological evidence of infectious virus is positive, including hepatitis B, hepatitis C, HIV and Treponema pallidum
Fasting C-peptide < 1.0 ng / ml (333 pmol / L)
Fertile eligible subjects (men and women) disagreed with the use of reliable contraceptive methods during the study and at least one month after the last administration
Pregnant or lactating women
Allergic to the active ingredient agratine hydrochloride, or severe allergic constitution / severe allergic history
Other circumstances judged by the sponsor or researcher as unsuitable for the study
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